Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 745–756 of 2,908 recalls
Downstream recall for RES 97605, BioPro femoral components. Product failed transit testing. Impacted product may have potential issues with sterile barrier.
Due to incorrect/lack of Unique Device Identifier (UDI) codes.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
Beckman Coulter has confirmed a software anomaly on DxI 9000 Access Immunoassay Analyzer and the DxC 500i Clinical Analyzer that may prevent correct application of user-specified manual dilution factors when ordering add…